ClinVar Miner

List of variants reported as benign for Mental retardation, X-linked, syndromic, Raymond type

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_016032.4(ZDHHC9):c.1033G>A (p.Glu345Lys) rs185917523
NM_016032.4(ZDHHC9):c.167+10G>A rs140526450
NM_016032.4(ZDHHC9):c.291G>A (p.Ala97=) rs77513704
NM_016032.4(ZDHHC9):c.626-10A>T rs188156112
NM_016032.4(ZDHHC9):c.674+9C>T rs376385410
NM_016032.4(ZDHHC9):c.975C>T (p.Ser325=) rs139619000

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.